510(k) K883526 ยท KNQ Dilator, Esophageal
PORGES STEPPED NEOPLEX DILATOR
| Applicant | Porges Corp., Gary IN, US |
| Decision | Substantially Equivalent, Oct 28, 1988 |
| Received | Aug 18, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883526
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.